1991
DOI: 10.1016/0024-3205(91)90053-e
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In vivo application of [111In-DTPA-D-Phe1]-octreotide for detection of somatostatin receptor-positive tumors in rats

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Cited by 156 publications
(82 citation statements)
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“…The use of tomography (SPECT) was reported to improve the detection of insulinomas: 80% were detected in a study about 14 patients with insulinoma (9). Pretreatment with octreotide might lead to saturation of somatostatin receptors (36).…”
Section: Discussionmentioning
confidence: 99%
“…The use of tomography (SPECT) was reported to improve the detection of insulinomas: 80% were detected in a study about 14 patients with insulinoma (9). Pretreatment with octreotide might lead to saturation of somatostatin receptors (36).…”
Section: Discussionmentioning
confidence: 99%
“…In-DTPAOctreotide, D-Phe-Cys-Phe-D-Trp-Lys-Thr-Cys-Thr[ol]), was successfully used to visualize somatostatin receptor positive tumors by gamma camera scintigraphy in the early 1990s [48][49][50] . Normal physiological uptake is seen in the thyroid, spleen, liver and pituitary due to receptor binding of the peptides, while tracer uptake in the kidneys is predominantly secondary to reabsorption of filtered peptides, and bowel uptake is presumably secondary to hepatobiliary clearance (Figures 6 and 7).…”
mentioning
confidence: 99%
“…Although SST-14 or SST-28 show binding to SSTR with similar affinity, the octapeptide analogs display high affinity to SSTR2 and SSTR5, moderate affinity to SSTR3, and have only poor binding to SSTR1 and SSTR4 (9,14,18). Based on the findings that various neuroendocrine malignancies and many other solid tumors such as breast, lung, renal, pancreatic, gastric, colon cancers, and brain tumors as well as androgenindependent metastatic adenocarcinoma of the prostate express SSTR2 and͞or SSTR5 (3,9,(13)(14)(15)(16)(17)(18)(19)(20)(21)(22), radiolabeled octapeptide analogs were designed for autoradiographic detection of such tumors and their metastases (3,7,23,24). Thus,…”
mentioning
confidence: 99%